A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925863



Internal ID22701090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14799892..14800486hg38UCSC Ensembl
chr12:14952826..14953420hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359105
Samples
Known GenesWBP11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925863
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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